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多发性结肠息肉病伴加德纳综合征和染色体镶嵌现象:一项家系分析

Multiple polyposis coli associated with Gardner's syndrome and chromosomal mosaicism: a family analysis.

作者信息

Dhaliwal M K, Hughes J I, Jackson G L, Pathak S

机构信息

Department of Cell Biology, University of Texas, M.D. Anderson Cancer Center, Houston.

出版信息

Am J Gastroenterol. 1990 Jul;85(7):880-3.

PMID:2164769
Abstract

A family in which the proband (father) has multiple polyposis coli associated with Gardner's syndrome and his only son, also with multiple polyps, has been studied cytogenetically. The karyotypes of the proband and the son have shown deletion in the short arm of one chromosome 12 in a small percentage of cells. Normal cells and cells with a deletion of a 12p were noted, not only in the lymphocytes, but also in the skin fibroblast culture of the son. The karyotypes of the asymptomatic mother and their unaffected daughter were considered to be normal.

摘要

一个家系中,先证者(父亲)患有与加德纳综合征相关的多发性结肠息肉病,他唯一的儿子也有多个息肉,已对其进行了细胞遗传学研究。先证者和儿子的核型显示,一小部分细胞中12号染色体短臂存在缺失。不仅在淋巴细胞中,而且在儿子的皮肤成纤维细胞培养物中,都发现了正常细胞和12号染色体短臂缺失的细胞。无症状母亲及其未受影响女儿的核型被认为是正常的。

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